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Cancers|June 20, 2019
Optimizing Genetic Workup in Pheochromocytoma and Paraganglioma by Integrating Diagnostic and Research ApproachesLaura Gieldon, Doreen William, Karl Hackmann, et al.
Cancer Research|March 18, 2016
An Epigenetic Reprogramming Strategy to Resensitize Radioresistant Prostate Cancer CellsClaudia Peitzsch, Monica Cojoc, Linda Hein, et al.
Gut|April 29, 2018
Human gastric cancer modelling using organoidsTherese Seidlitz, Sebastian R Merker, Alexander Rothe, et al.
Stem Cell Reports|January 24, 2018
Isogenic FUS-eGFP iPSC Reporter Lines Enable Quantification of FUS Stress Granule Pathology that Is Rescued by Drugs Inducing AutophagyLara Marrone, Ina Poser, Ian Casci, et al.
Cancers|January 1, 2020
Mutant IDH1 Differently Affects Redox State and Metabolism in Glial Cells of Normal and Tumor OriginJulia Biedermann, Matthias Preussler, Marina Conde, et al.
Plos One|March 26, 2013
A novel, diffusely infiltrative xenograft model of human anaplastic oligodendroglioma with mutations in FUBP1, CIC, and IDH1Barbara Klink, Hrvoje Miletic, Daniel Stieber, et al.
Cold Spring Harbor Molecular Case Studies|March 6, 2019
Response to olaparib in a <i>PALB2</i> germline mutated prostate cancer and genetic events associated with resistancePeter Horak, Joachim Weischenfeldt, Gunhild von Amsberg, et al.
European Journal of Human Genetics : EJHG|June 9, 2026
Hereditary cancer: Germline testing practices across ERN GENTURIS member countriesMilena Kiljańczyk, Zanda Daneberga, Mikk Tooming, et al.
Journal of Medical Genetics|February 5, 2016
Mutations in EXOSC2 are associated with a novel syndrome characterised by retinitis pigmentosa, progressive hearing loss, premature ageing, short stature, mild intellectual disability and distinctive gestaltNataliya Di Donato, Teresa Neuhann, Anne-Karin Kahlert, et al.
Plos Genetics|August 10, 2016
Identification and Functional Testing of ERCC2 Mutations in a Multi-national Cohort of Patients with Familial Breast- and Ovarian CancerAndreas Rump, Anna Benet-Pages, Steffen Schubert, et al.
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